Clinical Trials on Sphingolipidoses

Total 377 results

    • NCT02416661
      Completed
      Conditions: Lysosomal Storage Diseases; Gaucher Disease; Sphingolipidoses
    • NCT00668564
      Terminated
      Conditions: Hurler's Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Sphingolipidoses; Krabbe Disease; Wolman's Disease; Niemann-Pick Disease Type B; Niemann-Pick Disease, Type C
    • NCT02993796
      Recruiting
      Conditions: Krabbe Disease
    • NCT00004294
      Completed
      Conditions: Gaucher's Disease
    • NCT00004293
      Unknown status
      Conditions: Gaucher's Disease
    • NCT00004488
      Completed
      Conditions: Gaucher's Disease; Osteopenia
    • NCT00004450
      Completed
      Conditions: Adrenoleukodystrophy
    • NCT00004418
      Terminated
      Conditions: Adrenoleukodystrophy
    • NCT02171104
      Recruiting
      Conditions: Mucopolysaccharidosis Disorders; Hurler Syndrome; Hunter Syndrome; Maroteaux Lamy Syndrome; Sly Syndrome; Alpha-Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Glycoprotein Metabolic Disorders; Sphingolipidoses; Recessive Leukodystrophies; Globoid Cell Leukodystrophy; Metachromatic Leukodystrophy; Niemann-Pick B; Niemann-Pick C Subtype 2; Sphingomyelin Deficiency; Peroxisomal Disorders; Adrenoleukodystrophy With Cerebral Involvement; Zellweger Syndrome; Neonatal Adrenoleukodystrophy; Infantile Refsum Disease; Acyl-CoA Oxidase Deficiency; D-Bifunctional Enzyme Deficiency; Multifunctional Enzyme Deficiency; Alpha-methylacyl-CoA Racmase Deficiency; Mitochondrial Neurogastrointestingal Encephalopathy; Severe Osteopetrosis; Hereditary Leukoencephalopathy With Axonal Spheroids (HDLS; CSF1R Mutation); Inherited Metabolic Disorders
    • NCT01963650
      Terminated
      Conditions: Lipid Metabolism Disorders; Metachromatic Leukodystrophy (MLD); Nervous System Diseases; Brain Diseases; Central Nervous System Diseases; Demyelinating Diseases; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Sphingolipidoses; Hereditary Central Nervous System Demyelinating Diseases; Metabolic Inborn Brain Diseases; Lysosomal Storage Diseases; Metabolic Diseases; Sulfatidosis
    • NCT01043640
      Completed
      Conditions: Mucopolysaccharidosis; Hurler Syndrome; Hunter Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Adrenoleukodystrophy (ALD); Krabbe Disease; Metachromatic Leukodystrophy (MLD); Sphingolipidoses; Peroxisomal Disorders
    • NCT04519749
      Recruiting
      Conditions: Fabry Disease
    • NCT03233841
      Completed
      Conditions: Farber Disease; Farber's Disease; Farber Lipogranulomatosis; Acid Ceramidase Deficiency; Ceramidase Deficiency; N-Laurylsphingosine Deacylase Deficiency; ASAH1 Mutation
    • NCT00351156
      Completed
      Conditions: Gaucher Disease
    • NCT00005900
      Unknown status
      Conditions: I Cell Disease; Fucosidosis; Globoid Cell Leukodystrophy; Adrenoleukodystrophy; Mannosidosis; Niemann-Pick Disease; Pulmonary Complications; Mucopolysaccharidosis I; Mucopolysaccharidosis VI; Metachromatic Leukodystrophy; Gaucher's Disease; Wolman Disease
    • NCT00004378
      Completed
      Conditions: Thrombocytopenia; Metachromatic Leukodystrophy; Fanconi's Anemia; Thalassemia Major; Pure Red-Cell Aplasia; Inborn Errors of Metabolism
    • NCT02231710
      Active, not recruiting
      Conditions: Primary Immune Deficiency Disorders; Hemophagocytic Lymphohistiocytosis; Inherited Bone Marrow Failure Syndrome; Hemoglobinopathies; Metabolic Disorders
    • NCT00004442
      Terminated
      Conditions: Infantile Refsum's Disease; Zellweger Syndrome; Bifunctional Enzyme Deficiency; Adrenoleukodystrophy
    • NCT04758130
      Recruiting
      Conditions: Metabolic Disease; Fabry Disease; Gaucher Disease; Pompe Disease; Mitochondrial Diseases
    • NCT04724083
      Recruiting
      Conditions: Fabry
    • NCT04721366
      Not yet recruiting
      Conditions: Gaucher Disease
    • NCT04718779
      Not yet recruiting
      Conditions: Gaucher Disease
    • NCT04713475
      Recruiting
      Conditions: GM1 Gangliosidosis; GM1 Gangliosidosis, Type I; GM1 Gangliosidosis, Type 2; Beta-Galactosidase-1 (GLB1) Deficiency
    • NCT04708301
      Recruiting
      Conditions: Fabry Disease
    • NCT04656600
      Not yet recruiting
      Conditions: Gaucher's Disease